Gene: PLCL2 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs115792481
rs115792481
PLCL2
1 3 16898659 intron variant G/T snv 4.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs116577908
rs116577908
PLCL2
4 3 17056907 intron variant A/G snv 7.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs143759545
rs143759545
PLCL2 ; LOC105376972
1 3 16884567 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2060597
rs2060597
PLCL2
1 3 16847490 intron variant T/C snv 3.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs73146904
rs73146904
PLCL2
3 3 16891490 intron variant G/A snv 9.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs9821630
rs9821630
PLCL2
2 3 16929446 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016